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5WAL image
Identification Of An Imidazopyridine Scaffold To Generate Potent And Selective Tyk2 Inhibitors That Demonstrate Activity In An In Vivo Psoriasis Model

5WEV image
Identification Of An Imidazopyridine Scaffold To Generate Potent And Selective Tyk2 Inhibitors That Demonstrate Activity In An In Vivo Psoriasis Model
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.85 Å Release Date: 2017-09-06
Classification: Transferase/Transferase Inhibitor
Ligands: 9ZS
Modified Residue(s): PTR

4MCM image
Human Sod1 C57S Mutant, As-Isolated
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.20 Å Release Date: 2014-08-27
Classification: OXIDOREDUCTASE
Ligands: ZN, SO4

4MCN image
Human Sod1 C57S Mutant, Metal-Free
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.60 Å Release Date: 2014-08-27
Classification: OXIDOREDUCTASE
Ligands: SO4

4GVJ image
Tyk2 (Jh1) In Complex With Adenosine Di-Phosphate
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.03 Å Release Date: 2013-08-14
Classification: HYDROLASE
Ligands: ADP, MG

4GFM image
Jak2 Kinase (Jh1 Domain) With 2,6-Dichloro-N-(2-Oxo-2,5-Dihydropyridin-4-Yl)Benzamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.30 Å Release Date: 2013-06-19
Classification: TRANSFERASE/TRANSFERASE INHIBITOR
Ligands: 0X2
Modified Residue(s): PTR

4GFO image
Tyk2 Kinase (Jh1 Domain) With 2,6-Dichloro-N-(2-Oxo-2,5-Dihydropyridin-4-Yl)Benzamide

4GIH image
Tyk2 (Jh1) In Complex With 2,6-Dichloro-N-{2-[(Cyclopropylcarbonyl)Amino]Pyridin-4-Yl}Benzamide

4GMY image
Jak2 Kinase (Jh1 Domain) In Complex With 2,6-Dichloro-N-{2-[(Cyclopropylcarbonyl)Amino]Pyridin-4-Yl}Benzamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.40 Å Release Date: 2013-06-19
Classification: TRANSFERASE/TRANSFERASE INHIBITOR
Ligands: 0X5
Modified Residue(s): PTR

4GII image
Tyk2 (Jh1) In Complex With 2,6-Dichloro-4-Cyano-N-{2-[(Cyclopropylcarbonyl)Amino]Pyridin-4-Yl}Benzamide

4GJ2 image
Tyk2 (Jh1) In Complex With 2,6-Dichloro-N-[2-({[(1R,2R)-2-Fluorocyclopropyl]Carbonyl}Amino)Pyridin-4-Yl]Benzamide

4GJ3 image
Tyk2 (Jh1) In Complex With 2,6-Dichloro-4-Cyano-N-[2-({[(1R,2R)-2-Fluorocyclopropyl]Carbonyl}Amino)Pyridin-4-Yl]Benzamide

2WL3 image
Crystal Structure Of Catechol 2,3-Dioxygenase
Organism: Rhodococcus sp. dk17
Method: X-RAY DIFFRACTION
Resolution:2.20 Å Release Date: 2010-09-01
Classification: OXIDOREDUCTASE
Ligands: FE, CA, GOL
Modified Residue(s): MSE

2WL9 image
Crystal Structure Of Catechol 2,3-Dioxygenase
Organism: Rhodococcus sp. dk17
Method: X-RAY DIFFRACTION
Resolution:1.90 Å Release Date: 2010-09-01
Classification: OXIDOREDUCTASE
Ligands: FE, MG, GOL, MBD

3A1J image
Crystal Structure Of The Human Rad9-Hus1-Rad1 Complex
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.50 Å Release Date: 2009-06-02
Classification: HYDROLASE/CELL CYCLE
Modified Residue(s): MSE

2ZU6 image
Crystal Structure Of The Eif4A-Pdcd4 Complex
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.80 Å Release Date: 2009-02-24
Classification: HYDROLASE
Ligands: EDO, ACY
Modified Residue(s): MSE

3EIO image
Crystal Structure Analysis Of Dppiv Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.00 Å Release Date: 2008-11-04
Classification: HYDROLASE
Ligands: AJH, NAG
Modified Residue(s): ASN

2OLE image
Crystal Structure Of Human Dipeptidyl Peptidase Iv (Dppiv) Complex With Cyclic Hydrazine Derivatives
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.40 Å Release Date: 2008-01-22
Classification: HYDROLASE
Ligands: KR2

2YT4 image
Crystal Structure Of Human Dgcr8 Core

1B49 image
Dcmp Hydroxymethylase From T4 (Phosphate-Bound)
Organism: Enterobacteria phage t4
Method: X-RAY DIFFRACTION
Resolution:2.30 Å Release Date: 1999-01-13
Classification: TRANSFERASE
Ligands: PO4
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